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miR-105-1水平降低与非小细胞肺癌患者的不良生存相关。

Reduced miR-105-1 levels are associated with poor survival of patients with non-small cell lung cancer.

作者信息

Lu Gaixia, Fu Da, Jia Chengyou, Chai Li, Han Yang, Liu Jin, Wu Tingmiao, Xie Ruting, Chang Zhengyan, Yang Huiqiong, Luo Pei, Lv Zhongwei, Yu Fei, Zhong Xiaojun, Ma Yushui

机构信息

Department of Nuclear Medicine, Shanghai Tenth People's Hospital, Tongji University School of Medicine, Shanghai 200072, P.R. China.

Department of Radiology, Translational Medicine Center and Medical Imaging Research Institute, Central Hospital of Baotou, Inner Mongolia Medical University, Baotou, Inner Mongolia Autonomous Region 014040, P.R. China.

出版信息

Oncol Lett. 2017 Dec;14(6):7842-7848. doi: 10.3892/ol.2017.7228. Epub 2017 Oct 19.

Abstract

Altered expression of microRNAs (miRNAs or miRs) contributes to lung carcinogenesis. The present study performed an analysis of differentially expressed miRNAs in different peripheral blood samples from patients with various diseases vs. controls using the Gene Expression Omnibus (GEO) database data, and assessed miR-105-1 expression in 32 normal lung and 142 non-small cell lung cancer (NSCLC) tissue samples using reverse transcription-quantitative polymerase chain reaction. Survival data were calculated using Kaplan-Meier curves and a log-rank test. The stepwise forward Cox regression model was performed for univariate and multivariate analyses of independent predictor of overall survival (OS) of patients. The data on and tissue microarray analyses of miRNA expression revealed reduced miR-105-1 expression in different types of human cancer, particularly in NSCLC. The level of miR-105-1 expression was confirmed to be downregulated in NSCLC tissues compared with that in normal lung tissues. Reduced miR-105-1 expression was associated with larger tumor size as well as poor OS and disease-free survival (DFS) of patients. Multivariate survival analysis demonstrated that reduced miR-105-1 expression and tumor size were independent predictors for OS of NSCLC patients. In conclusion, reduced miR-105-1 expression in NSCLC tissues is associated with poor OS and DFS of NSCLC patients.

摘要

微小RNA(miRNA或miR)表达的改变有助于肺癌的发生。本研究利用基因表达综合数据库(GEO)的数据,对患有各种疾病的患者与对照组不同外周血样本中差异表达的miRNA进行了分析,并采用逆转录定量聚合酶链反应评估了32例正常肺组织和142例非小细胞肺癌(NSCLC)组织样本中miR-105-1的表达。使用Kaplan-Meier曲线和对数秩检验计算生存数据。对患者总生存期(OS)的独立预测因素进行单变量和多变量分析,采用逐步向前Cox回归模型。miRNA表达的芯片数据和组织微阵列分析显示,miR-105-1在不同类型的人类癌症中表达降低,尤其是在NSCLC中。与正常肺组织相比,NSCLC组织中miR-105-1的表达水平被证实下调。miR-105-1表达降低与肿瘤体积较大以及患者较差的OS和无病生存期(DFS)相关。多变量生存分析表明,miR-105-1表达降低和肿瘤大小是NSCLC患者OS的独立预测因素。总之,NSCLC组织中miR-105-1表达降低与NSCLC患者较差的OS和DFS相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b82/5755234/2611d7921b5c/ol-14-06-7842-g00.jpg

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